Canonical Allele Identifier: CA2687741690
Gene: FABP4 HGNC NCBI

Linked Data

gnomAD v4: 8-81478697-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478697C>A , CM000670.2:g.81478697C>A GRCh38
NC_000008.10:g.82390932C>A , CM000670.1:g.82390932C>A GRCh37
NC_000008.9:g.82553487C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256104.5:c.*168G>T MANE Select ENSP00000256104.4:n.*168G>T
ENST00000256104.4:c.*168G>T ENSP00000256104.4:n.*168G>T
ENST00000518669.5:n.502G>T
NM_001442.2:c.*168G>T NP_001433.1:n.*168G>T
XR_001745980.1:n.514+16723C>A
NM_001442.3:c.*168G>T MANE Select NP_001433.1:n.*168G>T